Immucor and Sirona Genomics Launch MIA FORA™ NGS HLA Typing Solution

Collaboration brings unique next generation sequencing solution to the HLA typing market

7 Jan 2016
Lois Manton-O'Byrne, PhD
Executive Editor

Product news

Immucor, Inc., a global leader in transfusion and transplantation diagnostics, in collaboration with Sirona Genomics, has announced the launch of MIA FORA NGS, a high resolution HLA typing solution that provides accurate, comprehensive coverage of 11 HLA genes. With an efficient workflow that can be uniquely automated or run manually, MIA FORA NGS is adapted for use on the Illumina MiSeq® next generation sequencing (NGS) platform and is now available research use only (RUO) in the US and other countries, with CE Mark anticipated shortly.

MIA FORA, which roughly translates from Greek to “once,” allows HLA laboratories to achieve high resolution matching with no need for secondary testing to resolve ambiguities – results in one pass. The MIA FORA NGS sample preparation kit for long-range PCR and library preparation is user friendly with all-in-one master mixes, one PCR set up protocol, one amplification condition for all genes and a unique gene balancing program. Users also have the option to automate front end sample handling – the only one system to offer this labor efficiency with a benchtop footprint, which also helps to reduce manual errors and optimize patient results.

The MIA FORA NGS analysis software is uniquely built from the ground up specifically for HLA NGS typing. With an intuitive user interface, the MIA FORA NGS software is the only available product using three algorithms for accurate genotyping calls, a proprietary database for accurate mapping and alignment, and a smart flagging system that enables users to make accurate allele calls rapidly.

“Sirona Genomics is excited to bring MIA FORA NGS to HLA laboratories around the world in collaboration with Immucor, a leader in transplant diagnostics,” stated Michael Mindrinos, Ph.D., President and co-founder of Sirona. “MIA FORA NGS enables users to realize the full power of NGS for HLA typing – marrying an easy-to-use sample preparation protocol with a proprietary bioinformatics solution. The result is higher resolution with less rework for the lab and a better matched donor for each patient.”

MIA FORA NGS provides superior whole gene coverage of all major HLA gene regions, including whole gene coverage for HLA-A,B, C, DPA1, DQA1, and DQB1; all exons and introns for HLA-DRB1,3,4,5 except partial coverage for exon 6 and intron 1; and all exons and introns between exons 2 and 4 for HLA-DPB1.

This announcement marks the first product release from the MIA FORA portfolio and complements Immucor’s LIFECODES transplant product family. A higher volume test kit for registry HLA typing is planned for 2016.

“Immucor is dedicated to ensuring patients in need of a transplant get the right match. Our MIA FORA NGS offering continues this commitment,” stated Keith Chaitoff, Chief Marketing Officer. “Our work with Sirona Genomics over the past 14 months has resulted in a superior product for the HLA laboratory, and the clinicians and patients they serve. And in this critical area of healthcare, patient care and quality of results must take priority. When combined with our LIFECODES transplant products, Immucor is able to provide a full range of solutions that meet the transplant community’s needs and delivers the accuracy transplant patients deserve.”

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Blood TransfusionBlood Transfusion involves giving donor blood to a recipient patient. Screening is essential to avoid transfusion reactions. Blood banks use immunohematological techniques to determine rh and ABO blood group, and screen for antibodies using specific antisera. Blood Banks use Direct Coombs Tests (DCT) and Indirect Coombs Tests (IAT) to detect hemolysis and Haemolytic Disease of the Newborn (HDN).Clinical GeneticsMolecular Genetics covers the analysis of hereditary genetic disease and chromosomal abnormalities. Genetics can be analysed using DNA, RNA, and protein microarrays, PCR, RT PCR and DNA sequencing. Genetic equipment includes genetic workstations, thermal cyclers, cooling blocks and electrophoresis products. Diagnostic kits are used for DNA / RNA extraction and purification.Chem / BioinformaticsCheminformatics and bioinformatics are computational techniques used in chemistry and biology, respectively, for data acquisition, processing and storage. Cheminformatics focuses on compound information, whereas bioinformatics is mainly applied to analysis and modeling of genomics, genetic and sequencing information. Hardware and software is available for data acquisition, analysis, management and storage.Sample PreparationSample preparation can improve the quality and speed of separation techniques. Products to assist sample preparation include filtration equipment, evaporators, membranes and sieves.DNA TypingPCR AutomationPCR automation describes the process of using a thermocycler to complete the polymerase chain reaction (PCR) process quickly and efficiently.Library PreparationLibrary preparation is a critical step in sequencing workflows, where DNA or RNA samples are converted into libraries for high-throughput, next generation sequencing. This step ensures accurate results and minimizes biases. Explore library preparation kits in our peer-reviewed product directory; compare products, check reviews, and get pricing directly from manufacturers.Molecular DiagnosticsMolecular diagnostics use an individual’s genetic code and gene expression to diagnose and monitor diseases. The technique is used increasingly in the field of infectious diseases and oncology, as well as areas such as coagulation, HLA typing and pharmacogenomics. Molecular diagnostics plays a pivotal role in personalized medicine.Clinical NGSNext Generation Sequencing (NGS) refers to the use of massive parallel sequencing of multiple small fragments of DNA. This high-throughput genomic analysis yields enormous amounts of sequence data, which if appropriately analyzed could have huge potential for clinical laboratories. For this to happen there are technique and bioinformatic hurdles to be overcome.